tert-butyl N-[(1S)-1-[[(1R)-1-[4-[(7-methoxy-2-phenyl-4-quinolyl)oxy]-3-vinyl-phenyl]-2-oxo-2-[[(1S)-1-[(2-vinylphenyl)sulfonylcarbamoyl]butyl]amino]ethyl]carbamoyl]-2,2-dimethyl-propyl]carbamate

InChIKey	`DIAWVOPAWLDFQK-ZVMKXMJESA-N`
Compound Name	tert-butyl N-[(1S)-1-[[(1R)-1-[4-[(7-methoxy-2-phenyl-4-quinolyl)oxy]-3-vinyl-phenyl]-2-oxo-2-[[(1S)-1-[(2-vinylphenyl)sulfonylcarbamoyl]butyl]amino]ethyl]carbamoyl]-2,2-dimethyl-propyl]carbamate
Canonical SMILES	`C=Cc1cc([C@@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(=O)N[C@@H](CCC)C(=O)NS(=O)(=O)c2ccccc2C=C)ccc1Oc1cc(-c2ccccc2)nc2cc(OC)ccc12`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	2
Pfam Stratification	Homologous
Avg pChEMBL	6.69
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
Q0ZMF1	NS3	Hepatitis C virus genotype 1b	Pathogen	PF02907	6.7	Ki	ChEMBL;BindingDB
C1KIQ2		Hepacivirus hominis	Pathogen	PF02907	6.6	Ki	ChEMBL